AbbVie Inc. is seeking a seasoned professional to lead global CMC submission activities for biologics, coordinating cross-functional teams to ensure high-quality regulatory documents.
The role emphasizes alignment with clinical development strategy and timely responses to authorities. Responsibilities include mentoring dossier authors, developing submission templates, and mitigating regulatory risks while maintaining strong external collaborations and internal leadership.
#J-18808-LjbffrGlobal CMC Dossier Strategy Lead in chicago at Unknown Company
This position is listed as full time and onsite.